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Destilla GmbH

FDA import alert and refusal historyNordlingen, GermanyFEI 3010115572

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Example subjectDestilla Gmb added to Import Alert 16-129 (red list)

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As of October 26, 2026, Destilla GmbH is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on December 24, 2019, most often for filthy, putrid or decomposed substance (FILTHY).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Tamarind (subtropical and tropical fruit) · FILTHY
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for Destilla GmbH

3 records, newest first. Each line links to the FDA page it came from.

2025

  1. Inspection
    Inspection classified NAI (No Action Indicated)Foodborne Biological Hazards
    Source

2019

  1. Import refusal
    Refused, 2 lines in one entry: Tamarind (subtropical and tropical fruit)FILTHYEntry 506-7504856-0Show 2 lines
    • Refused, Tamarind (subtropical and tropical fruit)FILTHYEntry 506-7504856-0Source
    • Refused, Tamarind (subtropical and tropical fruit)FILTHYEntry 506-7504856-0Source
    Source

Refusal charges, in plain English

  • FILTHY2 refused lines

    Filthy, putrid or decomposed substance

    The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.

Questions about Destilla GmbH

Is Destilla GmbH on an FDA import alert?
No listing for Destilla GmbH appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Germany page.
Has FDA refused shipments from Destilla GmbH?
Yes. FDA refused 2 shipment lines from Destilla GmbH on December 24, 2019. The most recent, on December 24, 2019, was tamarind (subtropical and tropical fruit), charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse Destilla GmbH's shipments?
The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 2 lines).
When was Destilla GmbH last inspected by FDA?
FDA's most recent inspection of Destilla GmbH with a final classification is dated June 20, 2025 and was classified NAI (No Action Indicated).
What is Destilla GmbH's FEI number?
Destilla GmbH's FDA Establishment Identifier (FEI) is 3010115572.

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Example subjectDestilla Gmb added to Import Alert 16-129 (red list)

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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.